CA2746600C - Binder compositions comprising boric acid or boric acid salt - Google Patents

Binder compositions comprising boric acid or boric acid salt Download PDF

Info

Publication number: CA2746600C
Authority: CA; Canada
Prior art keywords: monomers; weight; binder composition; boric acid; adhesive
Prior art date: 2008-12-22
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CA2746600A

Other languages

English (en)

French (fr)

Other versions

CA2746600A1 (en

Inventor

Alexandre Terrenoire

Frank Reinhold

Stephan Amthor

Michael Gross

Konrad Roschmann

Stefan Becker

Kamesh Vyakaranam

Jens Hartig

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

BASF SE

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2008-12-22

Filing date

2009-12-21

Publication date

2016-09-13

2009-12-21 Application filed by BASF SE filed Critical BASF SE

2010-07-01 Publication of CA2746600A1 publication Critical patent/CA2746600A1/en

2016-09-13 Application granted granted Critical

2016-09-13 Publication of CA2746600C publication Critical patent/CA2746600C/en

Status Expired - Fee Related legal-status Critical Current

2029-12-21 Anticipated expiration legal-status Critical

Links

239000000203 mixture Substances 0.000 title claims abstract description 144
239000011230 binding agent Substances 0.000 title claims abstract description 88
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 title claims abstract description 61
239000004327 boric acid Substances 0.000 title claims abstract description 59
239000000178 monomer Substances 0.000 claims abstract description 189
229920000642 polymer Polymers 0.000 claims abstract description 106
150000003839 salts Chemical class 0.000 claims abstract description 46
239000004815 dispersion polymer Substances 0.000 claims abstract description 27
239000002245 particle Substances 0.000 claims abstract description 23
230000009477 glass transition Effects 0.000 claims abstract description 18
229920003176 water-insoluble polymer Polymers 0.000 claims abstract description 18
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 13
238000010526 radical polymerization reaction Methods 0.000 claims abstract description 10
230000007935 neutral effect Effects 0.000 claims abstract description 9
238000004519 manufacturing process Methods 0.000 claims abstract description 4
230000001070 adhesive effect Effects 0.000 claims description 111
239000000853 adhesive Substances 0.000 claims description 110
-1 vinylaromatics Chemical class 0.000 claims description 109
239000006185 dispersion Substances 0.000 claims description 72
238000000576 coating method Methods 0.000 claims description 69
239000011248 coating agent Substances 0.000 claims description 59
239000000463 material Substances 0.000 claims description 45
239000007787 solid Substances 0.000 claims description 29
150000002763 monocarboxylic acids Chemical class 0.000 claims description 28
238000007720 emulsion polymerization reaction Methods 0.000 claims description 27
239000002253 acid Substances 0.000 claims description 25
239000004568 cement Substances 0.000 claims description 17
150000001991 dicarboxylic acids Chemical class 0.000 claims description 16
229910052783 alkali metal Inorganic materials 0.000 claims description 14
150000002148 esters Chemical class 0.000 claims description 14
239000000843 powder Substances 0.000 claims description 14
238000002360 preparation method Methods 0.000 claims description 12
150000003973 alkyl amines Chemical class 0.000 claims description 11
150000003863 ammonium salts Chemical class 0.000 claims description 10
125000005518 carboxamido group Chemical group 0.000 claims description 9
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 8
238000001035 drying Methods 0.000 claims description 8
125000005210 alkyl ammonium group Chemical group 0.000 claims description 7
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 7
150000001470 diamides Chemical class 0.000 claims description 7
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
150000001735 carboxylic acids Chemical class 0.000 claims description 6
150000003140 primary amides Chemical class 0.000 claims description 6
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 4
150000001408 amides Chemical class 0.000 claims description 4
150000005690 diesters Chemical class 0.000 claims description 4
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 3
238000005299 abrasion Methods 0.000 claims description 3
125000005907 alkyl ester group Chemical group 0.000 claims description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
230000000903 blocking effect Effects 0.000 claims description 2
238000000034 method Methods 0.000 abstract description 30
239000003431 cross linking reagent Substances 0.000 abstract description 5
238000006116 polymerization reaction Methods 0.000 description 48
229940117913 acrylamide Drugs 0.000 description 40
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 37
239000003995 emulsifying agent Substances 0.000 description 37
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
239000000243 solution Substances 0.000 description 34
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 33
238000012360 testing method Methods 0.000 description 27
238000009472 formulation Methods 0.000 description 24
229910001868 water Inorganic materials 0.000 description 23
238000005260 corrosion Methods 0.000 description 21
230000007797 corrosion Effects 0.000 description 21
239000000049 pigment Substances 0.000 description 21
229910021538 borax Inorganic materials 0.000 description 19
239000000945 filler Substances 0.000 description 19
235000010339 sodium tetraborate Nutrition 0.000 description 19
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 18
230000008569 process Effects 0.000 description 18
239000004328 sodium tetraborate Substances 0.000 description 18
239000000758 substrate Substances 0.000 description 18
229910052739 hydrogen Inorganic materials 0.000 description 17
239000001257 hydrogen Substances 0.000 description 17
125000004432 carbon atom Chemical group C* 0.000 description 15
239000003973 paint Substances 0.000 description 15
125000000217 alkyl group Chemical group 0.000 description 14
238000004132 cross linking Methods 0.000 description 14
BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 13
239000002562 thickening agent Substances 0.000 description 12
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
239000000654 additive Substances 0.000 description 11
239000000839 emulsion Substances 0.000 description 11
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 10
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
150000001642 boronic acid derivatives Chemical class 0.000 description 10
239000013530 defoamer Substances 0.000 description 10
239000003112 inhibitor Substances 0.000 description 10
238000003860 storage Methods 0.000 description 10
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
125000000129 anionic group Chemical group 0.000 description 9
239000000126 substance Substances 0.000 description 9
150000007513 acids Chemical class 0.000 description 8
239000003139 biocide Substances 0.000 description 8
230000000052 comparative effect Effects 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
239000000835 fiber Substances 0.000 description 8
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 8
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
239000003999 initiator Substances 0.000 description 7
239000003505 polymerization initiator Substances 0.000 description 7
239000011734 sodium Substances 0.000 description 7
159000000000 sodium salts Chemical class 0.000 description 7
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
239000013543 active substance Substances 0.000 description 6
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
230000003115 biocidal effect Effects 0.000 description 6
238000004332 deodorization Methods 0.000 description 6
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
238000009826 distribution Methods 0.000 description 6
229910052500 inorganic mineral Inorganic materials 0.000 description 6
238000005259 measurement Methods 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
235000010755 mineral Nutrition 0.000 description 6
239000011707 mineral Substances 0.000 description 6
239000011347 resin Substances 0.000 description 6
229920005989 resin Polymers 0.000 description 6
238000003756 stirring Methods 0.000 description 6
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
239000002671 adjuvant Substances 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
230000032798 delamination Effects 0.000 description 5
238000001704 evaporation Methods 0.000 description 5
230000008020 evaporation Effects 0.000 description 5
239000001023 inorganic pigment Substances 0.000 description 5
239000000123 paper Substances 0.000 description 5
230000002441 reversible effect Effects 0.000 description 5
238000005096 rolling process Methods 0.000 description 5
239000007921 spray Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
238000002834 transmittance Methods 0.000 description 5
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
235000011114 ammonium hydroxide Nutrition 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
239000011575 calcium Substances 0.000 description 4
239000008199 coating composition Substances 0.000 description 4
239000000084 colloidal system Substances 0.000 description 4
230000001143 conditioned effect Effects 0.000 description 4
239000000470 constituent Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000011156 evaluation Methods 0.000 description 4
150000002191 fatty alcohols Chemical class 0.000 description 4
238000009408 flooring Methods 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
239000011256 inorganic filler Substances 0.000 description 4
229910003475 inorganic filler Inorganic materials 0.000 description 4
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000011505 plaster Substances 0.000 description 4
230000001681 protective effect Effects 0.000 description 4
239000012966 redox initiator Substances 0.000 description 4
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000000454 talc Substances 0.000 description 4
229910052623 talc Inorganic materials 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 3
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
239000004971 Cross linker Substances 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 3
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
125000005250 alkyl acrylate group Chemical group 0.000 description 3
229910021529 ammonia Inorganic materials 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
238000013103 analytical ultracentrifugation Methods 0.000 description 3
235000010323 ascorbic acid Nutrition 0.000 description 3
229960005070 ascorbic acid Drugs 0.000 description 3
239000011668 ascorbic acid Substances 0.000 description 3
239000002585 base Substances 0.000 description 3
230000008901 benefit Effects 0.000 description 3
230000003247 decreasing effect Effects 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
230000003993 interaction Effects 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920000058 polyacrylate Polymers 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 3
235000010262 sodium metabisulphite Nutrition 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000002966 varnish Substances 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
239000002023 wood Substances 0.000 description 3
125000000923 (C1-C30) alkyl group Chemical group 0.000 description 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 description 2
PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
WFYBYTMONXCPBQ-UHFFFAOYSA-N 2-(2-oxoimidazolidin-1-yl)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCN1CCNC1=O WFYBYTMONXCPBQ-UHFFFAOYSA-N 0.000 description 2
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical class OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
XDVOLDOITVSJGL-UHFFFAOYSA-N 3,7-dihydroxy-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B(O)OB2OB(O)OB1O2 XDVOLDOITVSJGL-UHFFFAOYSA-N 0.000 description 2
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
240000002989 Euphorbia neriifolia Species 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
239000013032 Hydrocarbon resin Substances 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
MZZSDCJQCLYLLL-UHFFFAOYSA-N Secalonsaeure A Natural products COC(=O)C12OC3C(CC1=C(O)CC(C)C2O)C(=CC=C3c4ccc(O)c5C(=O)C6=C(O)CC(C)C(O)C6(Oc45)C(=O)OC)O MZZSDCJQCLYLLL-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
239000005083 Zinc sulfide Substances 0.000 description 2
230000009471 action Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000004035 construction material Substances 0.000 description 2
MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
FDENMIUNZYEPDD-UHFFFAOYSA-L disodium [2-[4-(10-methylundecyl)-2-sulfonatooxyphenoxy]phenyl] sulfate Chemical compound [Na+].[Na+].CC(C)CCCCCCCCCc1ccc(Oc2ccccc2OS([O-])(=O)=O)c(OS([O-])(=O)=O)c1 FDENMIUNZYEPDD-UHFFFAOYSA-L 0.000 description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
125000001033 ether group Chemical group 0.000 description 2
238000010528 free radical solution polymerization reaction Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
229940050410 gluconate Drugs 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229920006270 hydrocarbon resin Polymers 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
SBGKURINHGJRFN-UHFFFAOYSA-N hydroxymethanesulfinic acid Chemical compound OCS(O)=O SBGKURINHGJRFN-UHFFFAOYSA-N 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
238000011835 investigation Methods 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
239000010985 leather Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
239000001095 magnesium carbonate Substances 0.000 description 2
235000014380 magnesium carbonate Nutrition 0.000 description 2
229910000021 magnesium carbonate Inorganic materials 0.000 description 2
239000002609 medium Substances 0.000 description 2
239000012528 membrane Substances 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
125000000896 monocarboxylic acid group Chemical group 0.000 description 2
238000000465 moulding Methods 0.000 description 2
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000002105 nanoparticle Substances 0.000 description 2
239000004745 nonwoven fabric Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000012071 phase Substances 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
150000003009 phosphonic acids Chemical class 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
238000003825 pressing Methods 0.000 description 2
238000012545 processing Methods 0.000 description 2
VSVCAMGKPRPGQR-UHFFFAOYSA-N propan-2-one;sulfurous acid Chemical compound CC(C)=O.OS(O)=O VSVCAMGKPRPGQR-UHFFFAOYSA-N 0.000 description 2
239000001054 red pigment Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
238000003892 spreading Methods 0.000 description 2
230000007480 spreading Effects 0.000 description 2
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
238000010345 tape casting Methods 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
150000005621 tetraalkylammonium salts Chemical class 0.000 description 2
239000004753 textile Substances 0.000 description 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
125000005208 trialkylammonium group Chemical group 0.000 description 2
150000003628 tricarboxylic acids Chemical class 0.000 description 2
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
150000004072 triols Chemical class 0.000 description 2
229910052984 zinc sulfide Inorganic materials 0.000 description 2
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 2
MQLPUOPZIBQSJG-UHFFFAOYSA-N (2-ethyl-3-hydroxyhexyl) 2-methylprop-2-enoate Chemical compound CCCC(O)C(CC)COC(=O)C(C)=C MQLPUOPZIBQSJG-UHFFFAOYSA-N 0.000 description 1
VGPBTNMZOCCNAK-UHFFFAOYSA-N (2-ethyl-3-hydroxyhexyl) prop-2-enoate Chemical compound CCCC(O)C(CC)COC(=O)C=C VGPBTNMZOCCNAK-UHFFFAOYSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 description 1
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
BSSNZUFKXJJCBG-OWOJBTEDSA-N (e)-but-2-enediamide Chemical compound NC(=O)\C=C\C(N)=O BSSNZUFKXJJCBG-OWOJBTEDSA-N 0.000 description 1
KBRJTGNCPIFGFI-AATRIKPKSA-N (e)-n,n,n',n'-tetramethylbut-2-enediamide Chemical compound CN(C)C(=O)\C=C\C(=O)N(C)C KBRJTGNCPIFGFI-AATRIKPKSA-N 0.000 description 1
BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 description 1
BHESNSCMWDQLMH-ZCXUNETKSA-N (z)-n,n'-di(nonyl)but-2-enediamide Chemical compound CCCCCCCCCNC(=O)\C=C/C(=O)NCCCCCCCCC BHESNSCMWDQLMH-ZCXUNETKSA-N 0.000 description 1
XINTXMCKJPIVMC-DQSJHHFOSA-N (z)-n,n'-di(tetradecyl)but-2-enediamide Chemical compound CCCCCCCCCCCCCCNC(=O)\C=C/C(=O)NCCCCCCCCCCCCCC XINTXMCKJPIVMC-DQSJHHFOSA-N 0.000 description 1
UZAADJYMLXAZEX-QPLCGJKRSA-N (z)-n,n'-di(tridecyl)but-2-enediamide Chemical compound CCCCCCCCCCCCCNC(=O)\C=C/C(=O)NCCCCCCCCCCCCC UZAADJYMLXAZEX-QPLCGJKRSA-N 0.000 description 1
CGDSXGVAJVNEME-WAYWQWQTSA-N (z)-n,n'-diethylbut-2-enediamide Chemical compound CCNC(=O)\C=C/C(=O)NCC CGDSXGVAJVNEME-WAYWQWQTSA-N 0.000 description 1
UAZWJFZZYAUSSW-ARJAWSKDSA-N (z)-n,n'-dimethylbut-2-enediamide Chemical compound CNC(=O)\C=C/C(=O)NC UAZWJFZZYAUSSW-ARJAWSKDSA-N 0.000 description 1
WOLOATKQQOJIGE-NXVVXOECSA-N (z)-n,n'-dioctylbut-2-enediamide Chemical compound CCCCCCCCNC(=O)\C=C/C(=O)NCCCCCCCC WOLOATKQQOJIGE-NXVVXOECSA-N 0.000 description 1
LGGLBESHUDPAEE-WAYWQWQTSA-N (z)-n,n'-dipropylbut-2-enediamide Chemical compound CCCNC(=O)\C=C/C(=O)NCCC LGGLBESHUDPAEE-WAYWQWQTSA-N 0.000 description 1
QVJHNCMLYLFOQC-FPLPWBNLSA-N (z)-n,n'-ditert-butylbut-2-enediamide Chemical compound CC(C)(C)NC(=O)\C=C/C(=O)NC(C)(C)C QVJHNCMLYLFOQC-FPLPWBNLSA-N 0.000 description 1
OLWOGCIWEBYFKD-KTKRTIGZSA-N (z)-n,n,n',n'-tetraethylbut-2-enediamide Chemical compound CCN(CC)C(=O)\C=C/C(=O)N(CC)CC OLWOGCIWEBYFKD-KTKRTIGZSA-N 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
125000005919 1,2,2-trimethylpropyl group Chemical group 0.000 description 1
125000005918 1,2-dimethylbutyl group Chemical group 0.000 description 1
KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
HUOBWFKCWUVATL-UHFFFAOYSA-N 1-butyl-2-ethenylbenzene Chemical compound CCCCC1=CC=CC=C1C=C HUOBWFKCWUVATL-UHFFFAOYSA-N 0.000 description 1
QOVCUELHTLHMEN-UHFFFAOYSA-N 1-butyl-4-ethenylbenzene Chemical compound CCCCC1=CC=C(C=C)C=C1 QOVCUELHTLHMEN-UHFFFAOYSA-N 0.000 description 1
DMADTXMQLFQQII-UHFFFAOYSA-N 1-decyl-4-ethenylbenzene Chemical compound CCCCCCCCCCC1=CC=C(C=C)C=C1 DMADTXMQLFQQII-UHFFFAOYSA-N 0.000 description 1
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
OAAZUWWNSYWWHG-UHFFFAOYSA-N 1-phenoxypropan-1-ol Chemical compound CCC(O)OC1=CC=CC=C1 OAAZUWWNSYWWHG-UHFFFAOYSA-N 0.000 description 1
AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 description 1
PFPUZMSQZJFLBK-UHFFFAOYSA-N 2-(2-oxoimidazolidin-1-yl)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCN1CCNC1=O PFPUZMSQZJFLBK-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 description 1
TURPNXCLLLFJAP-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl hydrogen sulfate Chemical compound OCCOCCOCCOS(O)(=O)=O TURPNXCLLLFJAP-UHFFFAOYSA-N 0.000 description 1
WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
SQVSEQUIWOQWAH-UHFFFAOYSA-N 2-hydroxy-3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid Chemical compound CC(=C)C(=O)OCC(O)CS(O)(=O)=O SQVSEQUIWOQWAH-UHFFFAOYSA-N 0.000 description 1
MAQHZPIRSNDMAT-UHFFFAOYSA-N 2-hydroxy-3-prop-2-enoyloxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)COC(=O)C=C MAQHZPIRSNDMAT-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
125000005916 2-methylpentyl group Chemical group 0.000 description 1
GQTFHSAAODFMHB-UHFFFAOYSA-N 2-prop-2-enoyloxyethanesulfonic acid Chemical compound OS(=O)(=O)CCOC(=O)C=C GQTFHSAAODFMHB-UHFFFAOYSA-N 0.000 description 1
GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 description 1
KFNGWPXYNSJXOP-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid Chemical compound CC(=C)C(=O)OCCCS(O)(=O)=O KFNGWPXYNSJXOP-UHFFFAOYSA-N 0.000 description 1
XHTOIFCGKIBYRK-UHFFFAOYSA-N 3-(carbamoylamino)-2-methylprop-2-enoic acid Chemical compound OC(=O)C(C)=CNC(N)=O XHTOIFCGKIBYRK-UHFFFAOYSA-N 0.000 description 1
ATBDZSAENDYQDW-UHFFFAOYSA-N 3-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(C=C)=C1 ATBDZSAENDYQDW-UHFFFAOYSA-N 0.000 description 1
JRCGLALFKDKSAN-UHFFFAOYSA-N 3-hydroxybutyl prop-2-enoate Chemical compound CC(O)CCOC(=O)C=C JRCGLALFKDKSAN-UHFFFAOYSA-N 0.000 description 1
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
JSDZSLGMRRSAHD-UHFFFAOYSA-N 3-methylbutan-2-ylcyclopropane Chemical compound CC(C)C(C)C1CC1 JSDZSLGMRRSAHD-UHFFFAOYSA-N 0.000 description 1
125000005917 3-methylpentyl group Chemical group 0.000 description 1
NYUTUWAFOUJLKI-UHFFFAOYSA-N 3-prop-2-enoyloxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCOC(=O)C=C NYUTUWAFOUJLKI-UHFFFAOYSA-N 0.000 description 1
UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
MAGFQRLKWCCTQJ-UHFFFAOYSA-N 4-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-N 0.000 description 1
YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 description 1
NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
ZMFWTUBNIJBJDB-UHFFFAOYSA-N 6-hydroxy-2-methylquinoline-4-carboxylic acid Chemical compound C1=C(O)C=CC2=NC(C)=CC(C(O)=O)=C21 ZMFWTUBNIJBJDB-UHFFFAOYSA-N 0.000 description 1
XFOFBPRPOAWWPA-UHFFFAOYSA-N 6-hydroxyhexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCO XFOFBPRPOAWWPA-UHFFFAOYSA-N 0.000 description 1
OCIFJWVZZUDMRL-UHFFFAOYSA-N 6-hydroxyhexyl prop-2-enoate Chemical compound OCCCCCCOC(=O)C=C OCIFJWVZZUDMRL-UHFFFAOYSA-N 0.000 description 1
OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
RMZIOVJHUJAAEY-UHFFFAOYSA-N Allyl butyrate Chemical compound CCCC(=O)OCC=C RMZIOVJHUJAAEY-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
125000005915 C6-C14 aryl group Chemical group 0.000 description 1
229910021532 Calcite Inorganic materials 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229910001335 Galvanized steel Inorganic materials 0.000 description 1
241000598860 Garcinia hanburyi Species 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
235000000177 Indigofera tinctoria Nutrition 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
229920002266 Pluriol® Polymers 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
UEKQGZQLUMSLNW-UHFFFAOYSA-N Propyl isome Chemical compound C1=C2C(C(=O)OCCC)C(C(=O)OCCC)C(C)CC2=CC2=C1OCO2 UEKQGZQLUMSLNW-UHFFFAOYSA-N 0.000 description 1
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
241000238370 Sepia Species 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
229910000004 White lead Inorganic materials 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
230000001133 acceleration Effects 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229940091181 aconitic acid Drugs 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
238000007718 adhesive strength test Methods 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910001413 alkali metal ion Inorganic materials 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
235000019826 ammonium polyphosphate Nutrition 0.000 description 1
229920001276 ammonium polyphosphate Polymers 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
FAWGZAFXDJGWBB-UHFFFAOYSA-N antimony(3+) Chemical compound [Sb+3] FAWGZAFXDJGWBB-UHFFFAOYSA-N 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000000149 argon plasma sintering Methods 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
UHHXUPJJDHEMGX-UHFFFAOYSA-K azanium;manganese(3+);phosphonato phosphate Chemical compound [NH4+].[Mn+3].[O-]P([O-])(=O)OP([O-])([O-])=O UHHXUPJJDHEMGX-UHFFFAOYSA-K 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
239000011324 bead Substances 0.000 description 1
125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
ANCSWRGBBLAEOS-QXMHVHEDSA-N bis(2,4,4-trimethylpentan-2-yl) (z)-but-2-enedioate Chemical compound CC(C)(C)CC(C)(C)OC(=O)\C=C/C(=O)OC(C)(C)CC(C)(C)C ANCSWRGBBLAEOS-QXMHVHEDSA-N 0.000 description 1
239000010951 brass Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229940093876 calcium carbonate / kaolin Drugs 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
229940018557 citraconic acid Drugs 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical group [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
QMCVOSQFZZCSLN-QXMHVHEDSA-N dihexyl (z)-but-2-enedioate Chemical compound CCCCCCOC(=O)\C=C/C(=O)OCCCCCC QMCVOSQFZZCSLN-QXMHVHEDSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
PQJYOOFQDXGDDS-ZCXUNETKSA-N dinonyl (z)-but-2-enedioate Chemical compound CCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCC PQJYOOFQDXGDDS-ZCXUNETKSA-N 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
CUKXIDNDOQQWQN-FLWNBWAVSA-N dipentadecyl (z)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCCCCCCCC CUKXIDNDOQQWQN-FLWNBWAVSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
FNMTVMWFISHPEV-WAYWQWQTSA-N dipropan-2-yl (z)-but-2-enedioate Chemical compound CC(C)OC(=O)\C=C/C(=O)OC(C)C FNMTVMWFISHPEV-WAYWQWQTSA-N 0.000 description 1
UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
AJFXNBUVIBKWBT-UHFFFAOYSA-N disodium;boric acid;hydrogen borate Chemical compound [Na+].[Na+].OB(O)O.OB(O)O.OB(O)O.OB([O-])[O-] AJFXNBUVIBKWBT-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000002612 dispersion medium Substances 0.000 description 1
238000007323 disproportionation reaction Methods 0.000 description 1
WBZKQQHYRPRKNJ-UHFFFAOYSA-N disulfurous acid Chemical compound OS(=O)S(O)(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-N 0.000 description 1
DYVHFPDDBMMBAX-DQSJHHFOSA-N ditetradecyl (z)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCCCCCCC DYVHFPDDBMMBAX-DQSJHHFOSA-N 0.000 description 1
DFKBFBPHOGVNGQ-QPLCGJKRSA-N ditridecyl (z)-but-2-enedioate Chemical compound CCCCCCCCCCCCCOC(=O)\C=C/C(=O)OCCCCCCCCCCCCC DFKBFBPHOGVNGQ-QPLCGJKRSA-N 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003344 environmental pollutant Substances 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
FAFWKDXOUWXCDP-UHFFFAOYSA-N ethenylurea Chemical compound NC(=O)NC=C FAFWKDXOUWXCDP-UHFFFAOYSA-N 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
OUGJKAQEYOUGKG-UHFFFAOYSA-N ethyl 2-methylidenebutanoate Chemical compound CCOC(=O)C(=C)CC OUGJKAQEYOUGKG-UHFFFAOYSA-N 0.000 description 1
PVBRSNZAOAJRKO-UHFFFAOYSA-N ethyl 2-sulfanylacetate Chemical compound CCOC(=O)CS PVBRSNZAOAJRKO-UHFFFAOYSA-N 0.000 description 1
DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000010433 feldspar Substances 0.000 description 1
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
239000008397 galvanized steel Substances 0.000 description 1
229940117709 gamboge Drugs 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 1
SBGKURINHGJRFN-UHFFFAOYSA-M hydroxymethanesulfinate Chemical compound OCS([O-])=O SBGKURINHGJRFN-UHFFFAOYSA-M 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
229940097275 indigo Drugs 0.000 description 1
COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
230000002427 irreversible effect Effects 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
RYZCLUQMCYZBJQ-UHFFFAOYSA-H lead(2+);dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Pb+2].[Pb+2].[Pb+2].[O-]C([O-])=O.[O-]C([O-])=O RYZCLUQMCYZBJQ-UHFFFAOYSA-H 0.000 description 1
125000002463 lignoceryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005644 linolenyl group Chemical group 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
229910001552 magnesium chloroborate Inorganic materials 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001404 mediated effect Effects 0.000 description 1
HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000003595 mist Substances 0.000 description 1
125000002757 morpholinyl group Chemical group 0.000 description 1
125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
PSEVJQWXSXEXBV-UHFFFAOYSA-N n-(2-ethyl-3-hydroxyhexyl)-2-methylprop-2-enamide Chemical compound CCCC(O)C(CC)CNC(=O)C(C)=C PSEVJQWXSXEXBV-UHFFFAOYSA-N 0.000 description 1
HKCACRNQBIKMJH-UHFFFAOYSA-N n-(2-ethyl-3-hydroxyhexyl)-n,2-dimethylprop-2-enamide Chemical compound CCCC(O)C(CC)CN(C)C(=O)C(C)=C HKCACRNQBIKMJH-UHFFFAOYSA-N 0.000 description 1
FRLGZIFHECKIMW-UHFFFAOYSA-N n-(2-ethyl-3-hydroxyhexyl)-n-methylprop-2-enamide Chemical compound CCCC(O)C(CC)CN(C)C(=O)C=C FRLGZIFHECKIMW-UHFFFAOYSA-N 0.000 description 1
WCRXDKIUMUFDBH-UHFFFAOYSA-N n-(2-ethyl-3-hydroxyhexyl)prop-2-enamide Chemical compound CCCC(O)C(CC)CNC(=O)C=C WCRXDKIUMUFDBH-UHFFFAOYSA-N 0.000 description 1
BSCJIBOZTKGXQP-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCO BSCJIBOZTKGXQP-UHFFFAOYSA-N 0.000 description 1
KJWDFJXMZXZWTC-UHFFFAOYSA-N n-(2-hydroxyethyl)-n,2-dimethylprop-2-enamide Chemical compound OCCN(C)C(=O)C(C)=C KJWDFJXMZXZWTC-UHFFFAOYSA-N 0.000 description 1
VYHUMZYFJVMWRC-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylprop-2-enamide Chemical compound OCCN(C)C(=O)C=C VYHUMZYFJVMWRC-UHFFFAOYSA-N 0.000 description 1
UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 0.000 description 1
OKPYIWASQZGASP-UHFFFAOYSA-N n-(2-hydroxypropyl)-2-methylprop-2-enamide Chemical compound CC(O)CNC(=O)C(C)=C OKPYIWASQZGASP-UHFFFAOYSA-N 0.000 description 1
CBKFVALOTATEAK-UHFFFAOYSA-N n-(2-hydroxypropyl)-n,2-dimethylprop-2-enamide Chemical compound CC(O)CN(C)C(=O)C(C)=C CBKFVALOTATEAK-UHFFFAOYSA-N 0.000 description 1
NHISOSFLESCFIC-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylprop-2-enamide Chemical compound CC(O)CN(C)C(=O)C=C NHISOSFLESCFIC-UHFFFAOYSA-N 0.000 description 1
IPGRTXQKFZCLJS-UHFFFAOYSA-N n-(2-hydroxypropyl)prop-2-enamide Chemical compound CC(O)CNC(=O)C=C IPGRTXQKFZCLJS-UHFFFAOYSA-N 0.000 description 1
MSLHRSMWXQOHNA-UHFFFAOYSA-N n-(3-hydroxybutyl)-2-methylprop-2-enamide Chemical compound CC(O)CCNC(=O)C(C)=C MSLHRSMWXQOHNA-UHFFFAOYSA-N 0.000 description 1
DPZOEVBTOWWZMS-UHFFFAOYSA-N n-(3-hydroxybutyl)-n,2-dimethylprop-2-enamide Chemical compound CC(O)CCN(C)C(=O)C(C)=C DPZOEVBTOWWZMS-UHFFFAOYSA-N 0.000 description 1
YXMYPOYILIWOID-UHFFFAOYSA-N n-(3-hydroxybutyl)prop-2-enamide Chemical compound CC(O)CCNC(=O)C=C YXMYPOYILIWOID-UHFFFAOYSA-N 0.000 description 1
ZTUGCJNAJJDKDC-UHFFFAOYSA-N n-(3-hydroxypropyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCCO ZTUGCJNAJJDKDC-UHFFFAOYSA-N 0.000 description 1
ZZGCWICUHCMQAR-UHFFFAOYSA-N n-(3-hydroxypropyl)-n-methylprop-2-enamide Chemical compound C=CC(=O)N(C)CCCO ZZGCWICUHCMQAR-UHFFFAOYSA-N 0.000 description 1
ZEMHQYNMVKDBFJ-UHFFFAOYSA-N n-(3-hydroxypropyl)prop-2-enamide Chemical compound OCCCNC(=O)C=C ZEMHQYNMVKDBFJ-UHFFFAOYSA-N 0.000 description 1
TVDRFWWLJYRVMV-UHFFFAOYSA-N n-(4-hydroxybutyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCCCO TVDRFWWLJYRVMV-UHFFFAOYSA-N 0.000 description 1
ZXXBIMBIJAGGEE-UHFFFAOYSA-N n-(4-hydroxybutyl)-n,2-dimethylprop-2-enamide Chemical compound CC(=C)C(=O)N(C)CCCCO ZXXBIMBIJAGGEE-UHFFFAOYSA-N 0.000 description 1
BXSWQEXQDJCZGM-UHFFFAOYSA-N n-(4-hydroxybutyl)-n-methylprop-2-enamide Chemical compound C=CC(=O)N(C)CCCCO BXSWQEXQDJCZGM-UHFFFAOYSA-N 0.000 description 1
YBWQZBVPWXXJKQ-UHFFFAOYSA-N n-(4-hydroxybutyl)prop-2-enamide Chemical compound OCCCCNC(=O)C=C YBWQZBVPWXXJKQ-UHFFFAOYSA-N 0.000 description 1
LWXPRCDPAOOWFU-UHFFFAOYSA-N n-(6-hydroxyhexyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCCCCCO LWXPRCDPAOOWFU-UHFFFAOYSA-N 0.000 description 1
UYTRHCPOBNOPCG-UHFFFAOYSA-N n-(6-hydroxyhexyl)-n,2-dimethylprop-2-enamide Chemical compound CC(=C)C(=O)N(C)CCCCCCO UYTRHCPOBNOPCG-UHFFFAOYSA-N 0.000 description 1
PSJKLCSUGFKSDR-UHFFFAOYSA-N n-(6-hydroxyhexyl)prop-2-enamide Chemical compound OCCCCCCNC(=O)C=C PSJKLCSUGFKSDR-UHFFFAOYSA-N 0.000 description 1
DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012875 nonionic emulsifier Substances 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
WOTPFVNWMLFMFW-ISLYRVAYSA-N para red Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=C(N(=O)=O)C=C1 WOTPFVNWMLFMFW-ISLYRVAYSA-N 0.000 description 1
HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
238000011056 performance test Methods 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-N peroxydisulfuric acid Chemical class OS(=O)(=O)OOS(O)(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-N 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
231100000719 pollutant Toxicity 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
150000003097 polyterpenes Chemical class 0.000 description 1
235000019828 potassium polyphosphate Nutrition 0.000 description 1
230000002028 premature Effects 0.000 description 1
150000003858 primary carboxamides Chemical class 0.000 description 1
UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
ZQMAPKVSTSACQB-UHFFFAOYSA-N prop-2-enyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC=C ZQMAPKVSTSACQB-UHFFFAOYSA-N 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000004945 silicone rubber Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000000176 sodium gluconate Substances 0.000 description 1
235000012207 sodium gluconate Nutrition 0.000 description 1
229940005574 sodium gluconate Drugs 0.000 description 1
229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
235000019830 sodium polyphosphate Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
PQVFIKHKSFZHLT-UHFFFAOYSA-M sodium;3-ethenylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC(C=C)=C1 PQVFIKHKSFZHLT-UHFFFAOYSA-M 0.000 description 1
XFTALRAZSCGSKN-UHFFFAOYSA-M sodium;4-ethenylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C(C=C)C=C1 XFTALRAZSCGSKN-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
235000013759 synthetic iron oxide Nutrition 0.000 description 1
238000009864 tensile test Methods 0.000 description 1
WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
KWXLCDNSEHTOCB-UHFFFAOYSA-J tetrasodium;1,1-diphosphonatoethanol Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P(=O)([O-])C(O)(C)P([O-])([O-])=O KWXLCDNSEHTOCB-UHFFFAOYSA-J 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000005691 triesters Chemical class 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
239000012855 volatile organic compound Substances 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
AOTOLWUBPXXSEV-UHFFFAOYSA-H zinc molybdenum(4+) diphosphate hydrate Chemical compound O.[Zn+2].[Mo+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O AOTOLWUBPXXSEV-UHFFFAOYSA-H 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Paints Or Removers (AREA)

CA2746600A 2008-12-22 2009-12-21 Binder compositions comprising boric acid or boric acid salt Expired - Fee Related CA2746600C (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
EP08172579.8		2008-12-22
EP08172579		2008-12-22
PCT/EP2009/067608 WO2010072697A1 (de)	2008-12-22	2009-12-21	Bindemittelzusammensetzungen, die borsäure oder borsäuresalz enthalten

Publications (2)

Publication Number	Publication Date
CA2746600A1 CA2746600A1 (en)	2010-07-01
CA2746600C true CA2746600C (en)	2016-09-13

Family

ID=42026329

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2746600A Expired - Fee Related CA2746600C (en)	2008-12-22	2009-12-21	Binder compositions comprising boric acid or boric acid salt

Country Status (10)

Country	Link
US (1)	US8329800B2 (pl)
EP (1)	EP2379603B1 (pl)
CN (1)	CN102325797B (pl)
AU (1)	AU2009331576B2 (pl)
BR (1)	BRPI0922390A2 (pl)
CA (1)	CA2746600C (pl)
ES (1)	ES2421234T3 (pl)
PL (1)	PL2379603T3 (pl)
PT (1)	PT2379603E (pl)
WO (1)	WO2010072697A1 (pl)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP2167595B1 (de)	2007-06-20	2012-08-15	Basf Se	Verfahren zum aufbringen von korrosionsschutzschichten auf metallische oberflächen
US9435120B2 (en) *	2013-03-13	2016-09-06	Homax Products, Inc.	Acoustic ceiling popcorn texture materials, systems, and methods
US10132082B2 (en)	2013-09-18	2018-11-20	Firestone Building Products Co., LLC	Peel and stick roofing membranes with cured pressure-sensitive adhesives
US10065394B2 (en)	2014-03-07	2018-09-04	Firestone Building Products Co., LLC	Roofing membranes with pre-applied, cured, pressure-sensitive seam adhesives
USD787326S1 (en)	2014-12-09	2017-05-23	Ppg Architectural Finishes, Inc.	Cap with actuator
JP6020615B2 (ja) *	2015-01-28	2016-11-02	日立化成株式会社	エネルギーデバイス用電極並びにエネルギーデバイス及リチウムイオン二次電池
WO2017165871A1 (en)	2016-03-25	2017-09-28	Firestone Building Products Co., LLC	Method of reroofing
US20200299965A1 (en)	2016-03-25	2020-09-24	Firestone Building Products Company, Llc	Fully-adhered roof system adhered and seamed with a common adhesive
US12006692B2 (en)	2016-03-25	2024-06-11	Holcim Technology Ltd	Fully-adhered roof system adhered and seamed with a common adhesive
US20200299966A1 (en)	2016-03-25	2020-09-24	Firestone Building Products Company, Llc	Fabric-Backed Roofing Membrane Composite
US11001735B2 (en)	2016-07-14	2021-05-11	Sika Technology Ag	Low emission aqueous dispersion adhesive
WO2020178754A1 (en) *	2019-03-04	2020-09-10	Navoday Sciences Private Limited	Anti-corrosive coatings based on acid-base reactions
TR2022002642A2 (tr) *	2022-02-24	2022-03-21	Ersin Yildirim	Dental uygulamalar i̇çi̇n mekani̇k dayanimi i̇yi̇leşti̇ri̇lmi̇ş anti̇bakteri̇yel özelli̇kte poli̇mer esasli malzeme
CN116144293B (zh) *	2022-12-02	2024-09-10	陕西延长石油（集团）有限责任公司	一种长链聚合物胶水的制备方法及其在油气田中的应用

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2837992A1 (de)	1978-08-31	1980-03-20	Wacker Chemie Gmbh	Verfahren zur herstellung von waessrigen aethylen-vinylchlorid-vinylacetat und/oder alkylacrylatcopolymerdispersionen mit uneinheitlicher teilchengroesseverteilung
US4544699A (en) *	1983-10-11	1985-10-01	Union Oil Company Of California	Composition for improved adhesion of vinylidene chloride latex to ionomer films
DE4419518A1 (de)	1994-06-03	1995-12-07	Basf Ag	Verfahren zur Herstellung einer wäßrigen Polymerisatdispersion
DE4435423A1 (de)	1994-10-04	1996-04-11	Basf Ag	Verfahren zur Herstellung einer wäßrigen Polymerisatdispersion
DE4435422A1 (de)	1994-10-04	1996-04-18	Basf Ag	Verfahren zur Herstellung einer wäßrigen Polymerisatdispersion
DE10011387A1 (de)	2000-03-09	2001-09-13	Basf Ag	Beschichtungsmassen auf Basis emissionsarmer Bindemittel
EP1419893A1 (en)	2002-11-18	2004-05-19	Agfa-Gevaert	Improved ink jet recording material
US7270853B2 (en)	2003-06-12	2007-09-18	National Starch And Chemical Investment Holding Corporation	Glass adhesion promoter
US7329705B2 (en) *	2005-05-03	2008-02-12	Celanese International Corporation	Salt-sensitive binder compositions with N-alkyl acrylamide and fibrous articles incorporating same
US20080214080A1 (en)	2007-03-01	2008-09-04	Barcomb Christopher S	Salt-sensitive binder composition with latex processing aid
CN101711269B (zh)	2007-06-11	2013-05-15	巴斯夫欧洲公司	防腐涂料
EP2167595B1 (de)	2007-06-20	2012-08-15	Basf Se	Verfahren zum aufbringen von korrosionsschutzschichten auf metallische oberflächen

2009
- 2009-12-21 WO PCT/EP2009/067608 patent/WO2010072697A1/de not_active Ceased
- 2009-12-21 PL PL09798924T patent/PL2379603T3/pl unknown
- 2009-12-21 EP EP09798924.8A patent/EP2379603B1/de not_active Not-in-force
- 2009-12-21 US US13/141,178 patent/US8329800B2/en not_active Expired - Fee Related
- 2009-12-21 PT PT97989248T patent/PT2379603E/pt unknown
- 2009-12-21 CA CA2746600A patent/CA2746600C/en not_active Expired - Fee Related
- 2009-12-21 ES ES09798924T patent/ES2421234T3/es active Active
- 2009-12-21 BR BRPI0922390A patent/BRPI0922390A2/pt not_active Application Discontinuation
- 2009-12-21 CN CN200980157303.1A patent/CN102325797B/zh not_active Expired - Fee Related
- 2009-12-21 AU AU2009331576A patent/AU2009331576B2/en not_active Ceased

Also Published As

Publication number	Publication date
AU2009331576B2 (en)	2014-11-13
EP2379603A1 (de)	2011-10-26
US8329800B2 (en)	2012-12-11
EP2379603B1 (de)	2013-05-01
US20110257302A1 (en)	2011-10-20
AU2009331576A1 (en)	2011-07-21
BRPI0922390A2 (pt)	2016-01-26
PL2379603T3 (pl)	2013-09-30
CA2746600A1 (en)	2010-07-01
WO2010072697A1 (de)	2010-07-01
CN102325797B (zh)	2014-02-12
PT2379603E (pt)	2013-07-10
ES2421234T3 (es)	2013-08-29
CN102325797A (zh)	2012-01-18

Legal Events

Date	Code	Title	Description
2015-01-13	EEER	Examination request	Effective date: 20141218
2021-10-12	MKLA	Lapsed	Effective date: 20210831
2022-10-07	MKLA	Lapsed	Effective date: 20191223

Publication	Publication Date	Title
AU2009331576B2 (en)	2014-11-13	Binder compositions comprising boric acid or boric acid salt
US6348528B1 (en)	2002-02-19	Aqueous polymer dispersion containing an emulsifier with phosphate groups
US9382442B2 (en)	2016-07-05	Aqueous binder compositions
CN103068933B (zh)	2016-02-10	水性粘合剂组合物
AU2012234476B2 (en)	2016-03-10	Aqueous multistage polymer dispersion, process for its preparation and use thereof as binder for coating substrates
US20110312240A1 (en)	2011-12-22	Aqueous binder compositions
US6610776B2 (en)	2003-08-26	Aqueous high gloss emulsion paint with long open time
CN111315832B (zh)	2025-06-17	水性聚合物分散体
RU2666896C2 (ru)	2018-09-13	Применение водной полимерной дисперсии в покрывающих средствах для повышения цветостойкости
US11292861B2 (en)	2022-04-05	Aqueous polymer dispersion
CN103201303A (zh)	2013-07-10	水性乳液聚合物、其制法和用途
AU2016411502B2 (en)	2021-07-29	Coating composition with improved liquid stain repellency
US20020161079A1 (en)	2002-10-31	Use of phosphate group-containing polymer dispersions as adhesives
WO2025125496A1 (en)	2025-06-19	Aqueous polymer latex of copolymers suitable as binder in waterborne coating compositions
KR20260048629A (ko)	2026-04-10	수계 코팅 조성물에서 결합제로서 적합한 공중합체의 수성 중합체 라텍스
JP2025538509A (ja)	2025-11-28	水系コーティング組成物中のバインダーとして適した膜形成コポリマーの水性ポリマーラテックス
CN120917060A (zh)	2025-11-07	适合作为水性涂料组合物中的粘合剂的成膜共聚物的水性聚合物胶乳